Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42907537C>T , CM000679.2:g.42907537C>T | GRCh38 |
| NC_000017.10:g.41059554C>T , CM000679.1:g.41059554C>T | GRCh37 |
| NC_000017.9:g.38313080C>T | NCBI36 |
| NG_011808.1:g.11740C>T , LRG_147:g.11740C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000151.4:c.355C>T MANE Select | NP_000142.2:p.His119Tyr |
| ENST00000253801.7:c.355C>T MANE Select | ENSP00000253801.1:p.His119Tyr |
| NM_000151.3:c.355C>T | NP_000142.2:p.His119Tyr |
| NM_001270397.1:c.341-63C>T | NP_001257326.1:n.341-63C>T |
| NM_001270397.2:c.341-63C>T | NP_001257326.1:n.341-63C>T |
| ENST00000253801.6:c.355C>T | ENSP00000253801.1:p.His119Tyr |
| ENST00000585489.1:c.355C>T | ENSP00000466202.1:p.His119Tyr |
| ENST00000592383.5:c.341-63C>T | ENSP00000465958.1:n.341-63C>T |